Company ยท US
R-Group Intl.
FDA 510(k) clearances and medical device recalls filed under this name, 1992 to 2000. Name variants (Inc, Corp, punctuation) are merged.
7510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Dec 13, 2000 | K001233 | ACTI-FLEX FLUID DELIVERY SYSTEM OR ACTI-FLEX F D S R-Group Intl. | FPA |
| Sep 18, 2000 | K001599 | ACTI-FLEX IV ADMINISTRATION SET R-Group Intl. | FPA |
| May 25, 2000 | K993777 | DISPOSABLE AND REUSABLE BALL AND LOOP ELECTRODES R-Group Intl. | HGI |
| Nov 28, 1995 | K952470 | ACTI-FLEX LOW, MEDIUM, RESCARE I, RESCARE II. R-Group Intl. | GCD |
| Sep 25, 1995 | K954035 | ACTI-FLEX ARTERIAL EXTENSION SET R-Group Intl. | CBT |
| Nov 10, 1994 | K940319 | R-GROUP INTERNATIONAL COILED LOW PRESSURE EXTENSION LINE R-Group Intl. | FPA |
| Jun 5, 1992 | K913267 | R-GROUP INTL. ONE WALL PUNCTURE NEEDLE R-Group Intl. | DRC |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||